Atlas FDA

PSA Cable

FDA 510(k) clearance K170815 · decided 2017-07-06

Clearance details

K-number
K170815
Device name
PSA Cable
Applicant
Boston Scientific Corporation
Decision
Substantially Equivalent
Date received
2017-03-17
Decision date
2017-07-06
Days to decision
111 days
Clearance type
Traditional
Product code
DTC
Device class
2
Regulation number
870.3630
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
St Paul, MN, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
PK-141 PATIENT CABLE (K083674)Biotronik, Inc.2009-04-01
SIGMA PACE EXTERNAL PACEMAKER ANALYZER MODEL #1000 (K011729)Dni Nevada, Inc.2001-08-30
MODEL 4810 ANALYZER OUTPUT ADAPTER (K002497)Pace Medical2000-10-10
EXTERNAL PACEMAKER ANALYZER, MODEL PMT 100 (K961582)North American Technical Services Corp.1996-11-08
EXTERNAL PACEMAKER ANALYZER MODEL PMA-1 (K903966)Bio-Tek Instruments, Inc.1991-06-19
MODEL 5311B A-V PACING SYSTEM ANALYZER (K910595)Medtronic Vascular1991-05-07
CPI MODEL 2215/SEAMED MODEL 3400 (K910223)Seamed Corp.1991-03-19
PK-55 ANDOVER MEDICAL PART #5455 LABEL CHANGE (K901332)Biotronik, GmbH & Co.1990-05-09
MEDTRONIC MODEL 5401B TEST CABLE (K896632)Medtronic Vascular1989-12-13
MEDTRONIC MODEL 5311B A-V PACING SYSTEM ANALYZER (K884331)Medtronic Vascular1989-01-10
PACER SENSING ANALYZER (PSA 100) (K882327)Oscor Medical Corp.1988-10-06
SEAMED MODEL 3000 (K860462)Seamed Corp.1986-08-19

Recalls involving this device

No recalls on record reference this clearance.

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